ofloxacin
Generic: ofloxacin otic
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
ofloxacin
Generic Name
ofloxacin otic
Labeler
remedyrepack inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
ofloxacin 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3984
Product ID
70518-3984_3f8f78f1-534a-08e7-e063-6294a90a6718
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216130
Listing Expiration
2026-12-31
Marketing Start
2024-01-14
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183984
Hyphenated Format
70518-3984
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ofloxacin (source: ndc)
Generic Name
ofloxacin otic (source: ndc)
Application Number
ANDA216130 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 5 mL in 1 BOTTLE, DROPPER (70518-3984-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["AURICULAR (OTIC)"], "spl_id": "3f8f78f1-534a-08e7-e063-6294a90a6718", "openfda": {"nui": ["N0000175937", "M0023650"], "unii": ["A4P49JAZ9H"], "rxcui": ["242446"], "spl_set_id": ["fe619d50-49bf-4fcc-9428-6108c45580eb"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE, DROPPER (70518-3984-0)", "package_ndc": "70518-3984-0", "marketing_start_date": "20240114"}], "brand_name": "ofloxacin", "product_id": "70518-3984_3f8f78f1-534a-08e7-e063-6294a90a6718", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "70518-3984", "generic_name": "ofloxacin otic", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ofloxacin", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "ANDA216130", "marketing_category": "ANDA", "marketing_start_date": "20240114", "listing_expiration_date": "20261231"}